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Quantitative determination of total and unbound paclitaxel in human plasma following Abraxane treatment

  1. Author:
    Gardner, E. R.
    Dahut, W.
    Figg, W. D.
  2. Author Address

    Dahut, William, Figg, William D.] NCI, Clin Pharmacol Program, Ctr Canc Res, Med Oncol Div, Bethesda, MD 20892 USA. [Gardner, Erin R.] NCI, SAIC Frederick Inc, Clin Pharmacol Program, Frederick, MD 21702 USA.
    1. Year: 2008
  1. Journal: Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences
    1. 862
    2. 1-2
    3. Pages: 213-218
  2. Type of Article: Article
  1. Abstract:

    A simple, rapid liquid chromatography/tandem mass spectrometric (LC-MS/MS) assay was developed and validated for the quantification of both unbound and total paclitaxel in plasma following treatment with Abraxane (ABI-007) or Taxol. Accurate and reproducible analysis of ABI-007, an albumin nanoparticle formulation of paclitaxel could not be achieved using previously published methodology designed for Taxol. The final validated method involved protein precipitation followed by vacuum filtration, in a 96-well format for rapid processing. The 4 min run employed gradient elution on a Waters SymmetryShield C8 (2.1 mm x 50 mm, 3.5 mu m) column, followed by tandem mass spectrometric detection, in electrospray positive mode. Calibrator samples were prepared daily with paclitaxel and analyzed with both ABI-007 and paclitaxel quality control samples. To measure unbound drug, sample preparation was preceded by ultrafiltration. The assay was linear over the range of 10-2500 ng/mL, with dilution providing measurement up to 50,000 ng/mL. Within-run and between-run precision for all QC samples was less than 5.0% and 10.4%, respectively. Accuracy was high, with deviation of less than 6.1% for all QCs. Measurement of unbound paclitaxel was precise (BRP and WRP <10%). (C) 2008 Elsevier B.V. All rights reserved.

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External Sources

  1. PMID: 18191625

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